Main Purpose To provide Medical Products manufacturing, packing operations and customers with a Quality Control analysis service so that process control, product quality, and current Good Manufacturing Practice (cGMP) requirements are satisfied. This is a day role working Monday to Friday 8 am to 4 pm with flexibility required to move into a shift role in 6-12 months depending on business requirements. Main Responsibilities To accurately analyze, validate and record results for samples from the medical products operation to ensure that production processes and final product quality is controlled within the agreed specification limits. To review and validate the analysis of other analysts in line with operating requirements. Prioritize work to ensure that business production, sales and customer support plans are achieved. Carry out investigation into any abnormal results and report to the Medical Quality Control Team Leader, production personnel, and/or the Quality Assurance department, as appropriate. Maintain the laboratory, processes and analysis equipment in line with full requirements of current Good Manufacturing Practice. Ensure all sample, analysis and testing work is carried out in full compliance with written procedures, cGMP and SHE standards. Qualifications Minimum: HNC/HND Chemistry. Desirable: Degree in Chemistry or related subject. Knowledge/ Experience Required Knowledge and experience of working to cGMP standards. Understanding of QC in the pharmaceutical industry. Experience of working in a QC laboratory preferably one working to cGMP standards. Full clean driving license